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Sanofi-aventis Announces Second Quarter 2009 Results
Date:7/29/2009

he lower legs, is complete.
  • The Phase III study evaluating xaliproden in the prevention of severe peripheral sensory neuropathy induced by oxaliplatin in patients with metastatic colorectal cancer did not attain its primary end point. It was therefore decided to discontinue development of this product. It has also been decided not to proceed with the development of AVE1625, a CB1 inhibitor, in schizophrenia, following a recent interim analysis of the Phase II CONNECT study.
  • Filings for approval: The submission for marketing approval in Thailand and Australia of Imojev(R) (single-dose vaccine against Japanese encephalitis), was filed in July. This innovative vaccine is intended to prevent this disease in children and adults in endemic Asian countries. Submission for marketing approval in the United States of Menactra(R) Toddler (for children aged 9-12 months) is scheduled for the second half of 2009. In the fourth quarter of 2009, sanofi-aventis expects to file an application for an extension to the indication for Plavix(R) in atrial fibrillation, based on the results of the ACTIVE-A study.
  • In addition, the results of various studies are due to be presented shortly at medical congresses:

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